Variant report

Variant	rs1355159
Chromosome Location	chr4:126338549-126338550
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:126319752..126321593-chr4:126337337..126339510,2	MCF-7	breast:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10010000	0.87[AFR][1000 genomes]
rs10021774	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10025691	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10025821	0.87[AFR][1000 genomes]
rs10031471	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10084893	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10857105	1.00[YRI][hapmap]
rs11098811	1.00[AFR][1000 genomes]
rs11932005	1.00[YRI][hapmap]
rs11941296	0.87[AFR][1000 genomes]
rs12640965	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs12650153	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs13144799	1.00[YRI][hapmap]
rs13144803	1.00[YRI][hapmap]
rs1395243	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs1396687	1.00[YRI][hapmap]
rs1506362	1.00[AFR][1000 genomes]
rs1509298	1.00[LWK][hapmap]
rs1509301	1.00[LWK][hapmap]
rs1553714	1.00[YRI][hapmap]
rs1848579	1.00[AFR][1000 genomes]
rs1983117	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2036724	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2135427	1.00[YRI][hapmap]
rs2135428	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs2135429	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2390835	1.00[LWK][hapmap];1.00[YRI][hapmap]
rs2390836	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2390837	1.00[AFR][1000 genomes]
rs2390839	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2390840	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs2390841	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs2893131	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs4508902	1.00[YRI][hapmap]
rs4585321	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs4605670	0.87[AFR][1000 genomes]
rs4834030	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs4834034	1.00[YRI][hapmap]
rs4834036	1.00[YRI][hapmap]
rs4834039	1.00[YRI][hapmap]
rs4834041	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs4834043	1.00[ASW][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs4834047	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs4996182	1.00[YRI][hapmap]
rs6534480	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs6534484	1.00[YRI][hapmap]
rs6534485	1.00[YRI][hapmap]
rs6816596	0.87[AFR][1000 genomes]
rs6833240	1.00[YRI][hapmap]
rs6851018	1.00[YRI][hapmap]
rs6851098	0.87[AFR][1000 genomes]
rs7656135	0.87[AFR][1000 genomes]
rs7661747	0.86[AFR][1000 genomes]
rs7661810	0.87[AFR][1000 genomes]
rs7667605	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs7668690	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs7675556	1.00[YRI][hapmap]
rs7683955	1.00[YRI][hapmap]
rs7699122	1.00[ASW][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs958415	1.00[YRI][hapmap]
rs958844	0.87[AFR][1000 genomes]
rs958845	1.00[YRI][hapmap]
rs963397	0.87[AFR][1000 genomes]
rs988314	1.00[ASW][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs988315	1.00[AFR][1000 genomes]
rs988863	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs988933	1.00[YRI][hapmap]
rs9968423	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9991326	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs9995153	1.00[AFR][1000 genomes]
rs9996895	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006068	chr4:126103233-126497467	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv830051	chr4:126234895-126403426	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv470070	chr4:126299145-126408586	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:126311800-126341800	Weak transcription	Fetal Heart	heart
2	chr4:126311800-126343600	Weak transcription	Fetal Stomach	stomach
3	chr4:126312000-126354400	Weak transcription	HSMM	muscle
4	chr4:126312200-126342800	Weak transcription	NHLF	lung
5	chr4:126316600-126354600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:126319000-126343800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:126320000-126343400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr4:126320200-126354400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:126320600-126344400	Weak transcription	Lung	lung
10	chr4:126324800-126344400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:126326400-126340800	Weak transcription	Gastric	stomach
12	chr4:126327000-126341800	Weak transcription	Right Ventricle	heart
13	chr4:126329000-126344000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:126329600-126344400	Weak transcription	Fetal Intestine Small	intestine
15	chr4:126329800-126341400	Weak transcription	NHDF-Ad	bronchial
16	chr4:126334600-126390400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr4:126335000-126343600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr4:126335000-126344000	Weak transcription	Brain Hippocampus Middle	brain
19	chr4:126335200-126342000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr4:126335200-126353200	Weak transcription	Psoas Muscle	Psoas
21	chr4:126335200-126400800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr4:126335400-126343400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr4:126335600-126339000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr4:126335800-126338600	Weak transcription	Primary hematopoietic stem cells	blood
25	chr4:126335800-126338600	Strong transcription	Stomach Smooth Muscle	stomach
26	chr4:126335800-126340200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr4:126335800-126340800	Strong transcription	Fetal Lung	lung
28	chr4:126336000-126338600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:126336000-126338600	Strong transcription	Aorta	Aorta
30	chr4:126336000-126338800	Strong transcription	Fetal Muscle Trunk	muscle
31	chr4:126336000-126339000	Strong transcription	Left Ventricle	heart
32	chr4:126336000-126341000	Strong transcription	Ovary	ovary
33	chr4:126336000-126341400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:126336000-126343400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:126336200-126338600	Strong transcription	Fetal Muscle Leg	muscle
36	chr4:126336200-126338600	Strong transcription	HUVEC	blood vessel
37	chr4:126336200-126338800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr4:126336400-126338800	Weak transcription	Brain Anterior Caudate	brain
39	chr4:126336400-126339000	Strong transcription	Fetal Kidney	kidney
40	chr4:126336400-126344400	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr4:126336800-126344400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr4:126336800-126351000	Weak transcription	Fetal Brain Male	brain
43	chr4:126337000-126364400	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr4:126337600-126338800	Strong transcription	Fetal Intestine Large	intestine
45	chr4:126337800-126341000	Weak transcription	Colon Smooth Muscle	Colon
46	chr4:126337800-126356000	Weak transcription	Adipose Nuclei	Adipose
47	chr4:126337800-126356600	Weak transcription	Liver	Liver
48	chr4:126338000-126338600	Strong transcription	Fetal Brain Female	brain
49	chr4:126338000-126342200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:126338200-126338800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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